Forum Discussion
RobertaH
11 years agoMember
Lymphoedema Action Alliance
The LAA is working to improve the availability of public lymphoedema treatment practitioners and treatment centers
And also to get treatment and garment costs included in Medicare. BCNA is a partn...
Jen_McD
11 years agoMember
Done! i.e. went to the site and registered. I have found it curiously and frustratingly hard to get support with my lymphoedema problem - the gp didn't want to know (or even take a look) and it took 3 visits to the clinic by the breast care nurse before doc would write a referral to a lympho practitioner. Specialist has since done great things with massage and referral for compression garments, but it is sad that people have to wait 7 (seven) months after referral for an assessment appointment at the city hospital. Much more needs to be done to make necessary treatment available, and to inform doctors of the condition's relevance.